NDC11 51316070712
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 51316-0707-12 | 51316-0707 |
| 51316-707-12 | 51316-707 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CVS Stomach Relief Ultra Strength | BISMUTH SUBSALICYLATE | CVS PHARMACY | a7fb56c5-9b34-48b8-a355-a16979a0aa7b | 2026-08-17 | Warnings | 51316-707-12 51316-707 51316070712 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.